Literature DB >> 8545851

Microbial transformation of beta-sitosterol and stigmasterol into 26-oxygenated derivatives.

G Ambrus1, E Ilköy, A Jekkel, G Horváth, Z Böcskei.   

Abstract

The genetically modified Mycobacterium sp. BCS 396 strain has been used to transform sterols with stigmastane side chain in order to obtain 26-oxidized metabolites. beta-Sitosterol (I) was transformed to 4-stigmasten-3-one (II), 26-hydroxy-4-stigmasten-3-one (III), and 3-oxo-4-stigmasten-26-oic acid (IV), while stigmasterol (V) was converted to 4,22-stigmastadien-3-one (VI), 6 beta-hydroxy-4,22-stigmastadien-3-one (VII), 26-hydroxy-4,22-stigmastadien-3-one (VIII), 3-oxo-4,22-stigmastadien-26-oic acid methyl ester (IX), and 3-oxo-1,4,22-stigmastatrien-26-oic acid methyl ester (X) with that strain. In both beta-sitosterol and stigmasterol, 26-oxidation generates the R-configuration on C-25.

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Year:  1995        PMID: 8545851     DOI: 10.1016/0039-128x(95)00077-4

Source DB:  PubMed          Journal:  Steroids        ISSN: 0039-128X            Impact factor:   2.668


  1 in total

1.  Constituents from Vigna vexillata and their anti-inflammatory activity.

Authors:  Yann-Lii Leu; Tsong-Long Hwang; Ping-Chung Kuo; Kun-Pei Liou; Bow-Shin Huang; Guo-Feng Chen
Journal:  Int J Mol Sci       Date:  2012-08-06       Impact factor: 6.208

  1 in total

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